ID: ALA2268753

Max Phase: Preclinical

Molecular Formula: C16H25N3OSi

Molecular Weight: 303.48

Molecule Type: Unknown

Associated Items:

Representations

Canonical SMILES:  Cc1ccc(C(O)(CC[Si](C)(C)C)Cn2cncn2)cc1

Standard InChI:  InChI=1S/C16H25N3OSi/c1-14-5-7-15(8-6-14)16(20,9-10-21(2,3)4)11-19-13-17-12-18-19/h5-8,12-13,20H,9-11H2,1-4H3

Standard InChI Key:  LHMRUHFTXKQVQU-UHFFFAOYSA-N

Associated Targets(non-human)

Blumeria hordei 55 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Rhizoctonia solani 2251 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Pyricularia grisea 1253 Activities

Activity TypeRelationActivity valueUnitsAction TypeJournalPubMed IddoiAssay Aladdin ID

Molecule Features

Natural Product: NoOral: NoChemical Probe: NoParenteral: No
Molecule Type: UnknownTopical: NoFirst In Class: NoBlack Box: No
Chirality: NoAvailability: NoProdrug: No

Drug Indications

MESH IDMESH Heading EFO IDsEFO TermsMax Phase for IndicationReferences

Mechanisms of Action

Mechanism of ActionAction Typetarget IDTarget NameTarget TypeTarget OrganismBinding Site NameReferences

Properties

Molecular Weight: 303.48Molecular Weight (Monoisotopic): 303.1767AlogP: #Rotatable Bonds:
Polar Surface Area: Molecular Species: HBA: HBD:
#RO5 Violations: HBA (Lipinski): HBD (Lipinski): #RO5 Violations (Lipinski):
CX Acidic pKa: CX Basic pKa: CX LogP: CX LogD:
Aromatic Rings: Heavy Atoms: QED Weighted: Np Likeness Score:

References

1. Itoh H, Yoneda R, Tobitsuka J, Ohta H, Takahi Y, Tsuda M, Takeshiba H..  (2003)  Synthesis of 1-triazolyl-4-trimethylsilyl-2-butanol and 1-triazolyl-5-trimethylsilyl-2-pentanol derivatives and an investigation of their fungicidal activities.,  51  (9): [PMID:12951461] [10.1248/cpb.51.1113]

Source